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Time series archives of remotely sensed data offer many possibilities to observe and analyse dynamic environmental processes at the Earth- surface. Based on these hypertemporal archives, which offer continuous observations of vegetation indices, typically at repetition rates from one to two weeks, sets of phenological parameters or metrics can be derived. Examples of such parameters are the beginning and end of the annual growing period, as well as its length. Even though these parameters do not correspond exactly to conventional observations of phenological events, they nevertheless provide indications of the dynamic processes occurring in the biosphere. The development of robust algorithms for the derivation of phenological metrics can be challenging. Currently, such algorithms are most commonly based on digital filters or the Fourier analysis of time series. Polynomial spline models offer a useful alternative to existing methods. The possibilities of using spline models in the analytical description of time series are numerous, and their specific mathematical properties may help to avoid known problems occurring with the more common methods for deriving phenological metrics. Based on a selection of different polynomial spline models suitable for the analysis of remotely sensed time series of vegetation indices, a method to derive various phenological parameters from such time series was developed and implemented in this work. Using an example data set from an intensively used agricultural area showing highly dynamic variations in vegetation phenology, the newly developed method was verified by a comparison of the results of the spline based approach to the results of two alternative, well established methods.

Magnet Resonance Imaging (MRI) and Electroencephalography (EEG) are tools used to investigate the functioning of the working brain in both humans and animal studies. Both methods are increasingly combined in separate or simultaneous measurements under the assumption to benefit from their individual strength while compensating their particular weaknesses. However, little attention has been paid to how statistical analyses strategies can influence the information that can be retrieved from a combined EEG fMRI study. Two independent studies in healthy student volunteers were conducted in the context of emotion research to demonstrate two approaches of combining MRI and EEG data of the same participants. The first study (N = 20) applied a visual search paradigm and found that in both measurements the assumed effects were absent by not statistically combining their results. The second study (N = 12) applied a novelty P300 paradigm and found that only the statistical combination of MRI and EEG measurements was able to disentangle the functional effects of brain areas involved in emotion processing. In conclusion, the observed results demonstrate that there are added benefits of statistically combining EEG-fMRI data acquisitions by assessing both the inferential statistical structure and the intra-individual correlations of the EEG and fMRI signal.

One of the main tasks in mathematics is to answer the question whether an equation possesses a solution or not. In the 1940- Thom and Glaeser studied a new type of equations that are given by the composition of functions. They raised the following question: For which functions Î¨ does the equation F(Î¨)=f always have a solution. Of course this question only makes sense if the right hand side f satisfies some a priori conditions like being contained in the closure of the space of all compositions with Î¨ and is easy to answer if F and f are continuous functions. Considering further restrictions to these functions, especially to F, extremely complicates the search for an adequate solution. For smooth functions one can already find deep results by Bierstone and Milman which answer the question in the case of a real-analytic function Î¨. This work contains further results for a different class of functions, namely those Î¨ that are smooth and injective. In the case of a function Î¨ of a single real variable, the question can be fully answered and we give three conditions that are both sufficient and necessary in order for the composition equation to always have a solution. Furthermore one can unify these three conditions to show that they are equivalent to the fact that Î¨ has a locally Hölder-continuous inverse. For injective functions Î¨ of several real variables we give necessary conditions for the composition equation to be solvable. For instance Î¨ should satisfy some form of local distance estimate for the partial derivatives. Under the additional assumption of the Whitney-regularity of the image of Î¨, we can give sufficient conditions for flat functions f on the critical set of Î¨ to possess a solution F(Î¨)=f.

Effective Elements on E-Marketing strategy in Tourism Industry (Case study Germany and Iran Airlines, Tour Operator and Chain Hotels) By: Seyed Siamak Mousavi Supervisor: Prof. Dr. Andreas Kagermeier This dissertation focuses on e-marketing strategy's effective elements in tourism industry. As case study, research focus is on Airlines, tour operator, chain hotels in Iran and Germany. It aims to show various possibilities to enhance the company- e-marketing strategy and successfully performance e-marketing strategies with recognition effective elements and their important during the strategy designing and implementation process. For the purpose of this research due to the nature of the research, Explanatory -exploratory-applicable; after studying and consulting, Delphi technique has been chosen. In results, we have some effective elements and their important according the Delphi and AHP method. For example between elements "Tourists' Needs, Experience and Expects" with the importance coefficient of %204 is the most remarkable elements and "Customer satisfactions' elements group" with average value 5.54 according the research results have more important than other groups.

In this thesis, in order to shed light on the biological function of the membrane-bound Glucocorticoid Receptor (mGR), proteomic changes induced by 15 min in vivo acute stress and by short in vitro activation of the mGR were analyzed in T-lymphocytes. The numerous overlaps between the two datasets suggest that the mGR mediates physiologically relevant actions and participates in the early stress response, triggering rapid early priming events that pave the way for the slower genomic GC activities. In addition, a new commercially available method with suitable sensitivity to detect the human mGR is reported and the transcriptional origin of this protein investigated. Our results indicates that specific GR-transcripts, containing exon 1C and 1D, are associated with the expression of this membrane isoform.

In this thesis, we mainly investigate geometric properties of optimal codebooks for random elements $X$ in a seperable Banach space $E$. Here, for a natural number $ N $ and a random element $X$ , an $N$-optimal codebook is an $ N $-subset in the underlying Banach space $E$ which gives a best approximation to $ X $ in an average sense. We focus on two types of geometric properties: The global growth behaviour (growing in $N$) for a sequence of $N$-optimal codebooks is described by the maximal (quantization) radius and a so-called quantization ball. For many distributions, such as central-symmetric distributions on $R^d$ as well as Gaussian distributions on general Banach spaces, we are able to estimate the asymptotics of the quantization radius as well as the quantization ball. Furthermore, we investigate local properties of optimal codebooks, in particular the local quantization error and the weights of the Voronoi cells induced by an optimal codebook. In the finite-dimensional setting, we are able to proof for many interesting distributions classical conjectures on the asymptotic behaviour of those properties. Finally, we propose a method to construct sequences of asymptotically optimal codebooks for random elements in infinite dimensional Banach spaces and apply this method to construct codebooks for stochastic processes, such as fractional Brownian Motions.

The main objective of the present thesis was to investigate whether antibody effects observed in earlier in vitro studies can translate into the protection against chemical carcinogenesis in vivo as the basis of an immunoprophylactic approach against carcinogens. As model for chemical carcinogenesis, we selected B[a]P the prototype polycyclic aromatic hydrocarbon (PAH), an environmental pollutant emanating from both natural and anthropogenic sources. Many in vivo models conveniently use high doses of carcinogens mostly given as single bolus, which provides simple surrogate readouts, but poorly reflects chronic exposure to the low concentrations found in the environment. In addition, these concentrations cannot be matched with equimolar antibody concentrations obtained by immunisation. However, low B[a]P concentrations do not permit to directly measure chemical carcinogenesis. Therefore, in the present thesis, the pharmacokinetic, metabolism and B[a]P mediated immunotoxicity were chosen as experimental read-outs. B[a]P conjugate vaccines based on ovalbumin, tetanus toxoid and diphtheria toxoid (DT) as carrier proteins were developed to actively immunise mice against B[a]P. B[a]P-DT conjugate induced the most robust immune response. The antibodies reacted not only with B[a]P but also with the proximate carcinogen 7,8-diol-B[a]P. Antibodies modulated the bioavailability of B[a]P and its metabolic activation in a dose-dependent manner by sequestration in the blood. In order to further improve the vaccination, we replaced the protein carrier by promiscuous T-helper cell epitopes to induce higher antibody titer with increased specificity for the B[a]P hapten. We hypothesised that a reduction of B cell binding sites on the carrier, compared to whole protein carrier, should favour the activation of B cells recognising the hapten instead of the carrier protein. An internal processing of the carrier and cleavage of the B[a]P-BA and subsequent presentation of the carrier peptide by MHC II molecules to T cell receptor should induce a B cell dependent immune response by activating B cells capable to recognise B[a]P. We demonstrated that a vaccination against B[a]P using promiscuous T-helper cell epitopes as a carrier is feasible and some tested peptide conjugates were more immunogenic as whole protein conjugates with increased specificity. We showed that vaccination against B[a]P reduces immunotoxicity. B[a]P suppressed the proliferative response of both T and B cells after a sub-acute administration, an effect that was completely reversed by vaccination. In immunized mice the immunotoxic effect of B[a]P on IFN-Î³, Il-12, TNF-ï¡ production and B cell activation was restored. In addition, specific antibodies inhibited the induction of Cyp1a1 by B[a]P in lymphocytes and Cyp1b1 in the liver, enzymes that are known to convert the procarcinogen B[a]P to the ultimate DNA-adduct forming metabolite, a major risk factor of chemical carcinogenesis. In order to replace Freund adjuvant and to improve the immunisation strategy in terms of antibody quantity and quality, several adjuvants that are potentially compatible with their use in humans were tested. In combination with Freund adjuvant, the conjugate-vaccine induced high levels of B[a]P-specific antibodies. We showed that all adjuvants tested induced specific antibodies against B[a]P and 7,8-diol-B[a]P, its carcinogenic metabolite. The highest antibody levels were obtained with Quil A, MF-59 and Alum. Biological activity in terms of enhanced retention of B[a]P was confirmed in mice immunised with Quil A, Montanide, Alum and MF-59. Our findings demonstrate that a vaccination against B[a]P is feasible in combination with adjuvants licensed in humans. Based on these results and with the current understanding of the mechanisms of chemical carcinogenesis of the ubiquitous carcinogen B[a]P and of the effects of specific antibodies, an immunoprophylactic approach against chemical carcinogenesis is absolutely warranted. Nevertheless, the direct effects of B[a]P-specific antibodies on the different stages of carcinogenesis (e.g. adduct formation) and whether these effects may translate into long-term protective effect against tumourigenesis needs to be proven in further experiments.

Arctic and Antarctic polynya systems are of high research interest since extensive new ice formation takes place in these regions. The monitoring of polynyas and the ice production is crucial with respect to the changing sea-ice regime. The thin-ice thickness (TIT) distribution within polynyas controls the amount of heat that is released to the atmosphere and has therefore an impact on the ice-production rates. This thesis presents an improved method to retrieve thermal-infrared thin-ice thickness distributions within polynyas. TIT with a spatial resolution of 1 km Ã— 1 km is calculated using the MODIS ice-surface temperature and atmospheric model variables within the Laptev Sea polynya for the winter periods 2007/08 and 2008/09. The improvement of the algorithm is focused on the surface-energy flux parameterizations. Furthermore, a thorough sensitivity analysis is applied to quantify the uncertainty in the thin-ice thickness results. An absolute mean uncertainty of -±4.7 cm for ice below 20 cm of thickness is calculated. Furthermore, advantages and drawbacks using different atmospheric data sets are investigated. Daily MODIS TIT composites are computed to fill the data gaps arising from clouds and shortwave radiation. The resulting maps cover on average 70 % of the Laptev Sea polynya. An intercomparison of MODIS and AMSR-E polynya data indicates that the spatial resolution issue is essential for accurately deriving polynya characteristics. Monthly fast-ice masks are generated using the daily TIT composites. These fast-ice masks are implemented into the coupled sea-ice/ocean model FESOM. An evaluation of FESOM sea-ice concentrations is performed with the result that a prescribed high-resolution fast-ice mask is necessary regarding the accurate polynya location. However, for a more realistic simulation of other small-scale sea-ice features further model improvements are required. The retrieval of daily high-resolution MODIS TIT composites is an important step towards a more precise monitoring of thin sea ice and sea-ice production. Future work will address a combined remote sensing " model assimilation method to simulate fully-covered thin-ice thickness maps that enable the retrieval of accurate ice production values.

Optimal control problems are optimization problems governed by ordinary or partial differential equations (PDEs). A general formulation is given byrn \min_{(y,u)} J(y,u) with subject to e(y,u)=0, assuming that e_y^{-1} exists and consists of the three main elements: 1. The cost functional J that models the purpose of the control on the system. 2. The definition of a control function u that represents the influence of the environment of the systems. 3. The set of differential equations e(y,u) modeling the controlled system, represented by the state function y:=y(u) which depends on u. These kind of problems are well investigated and arise in many fields of application, for example robot control, control of biological processes, test drive simulation and shape and topology optimization. In this thesis, an academic model problem of the form \min_{(y,u)} J(y,u):=\min_{(y,u)}\frac{1}{2}\|y-y_d\|^2_{L^2(\Omega)}+\frac{\alpha}{2}\|u\|^2_{L^2(\Omega)} subject to -\div(A\grad y)+cy=f+u in \Omega, y=0 on \partial\Omega and u\in U_{ad} is considered. The objective is tracking type with a given target function y_d and a regularization term with parameter \alpha. The control function u takes effect on the whole domain \Omega. The underlying partial differential equation is assumed to be uniformly elliptic. This problem belongs to the class of linear-quadratic elliptic control problems with distributed control. The existence and uniqueness of an optimal solution for problems of this type is well-known and in a first step, following the paradigm 'first optimize, then discretize', the necessary and sufficient optimality conditions are derived by means of the adjoint equation which ends in a characterization of the optimal solution in form of an optimality system. In a second step, the occurring differential operators are approximated by finite differences and the hence resulting discretized optimality system is solved with a collective smoothing multigrid method (CSMG). In general, there are several optimization methods for solving the optimal control problem: an application of the implicit function theorem leads to so-called black-box approaches where the PDE-constrained optimization problem is transformed into an unconstrained optimization problem and the reduced gradient for these reduced functional is computed via the adjoint approach. Another possibilities are Quasi-Newton methods, which approximate the Hessian by a low-rank update based on gradient evaluations, Krylov-Newton methods or (reduced) SQP methods. The use of multigrid methods for optimization purposes is motivated by its optimal computational complexity, i.e. the number of required computer iterations scales linearly with the number of unknowns and the rate of convergence, which is independent of the grid size. Originally multigrid methods are a class of algorithms for solving linear systems arising from the discretization of partial differential equations. The main part of this thesis is devoted to the investigation of the implementability and the efficiency of the CSMG on commodity graphics cards. GPUs (graphic processing units) are designed for highly parallelizable graphics computations and possess many cores of SIMD-architecture, which are able to outperform the CPU regarding to computational power and memory bandwidth. Here they are considered as prototype for prospective multi-core computers with several hundred of cores. When using GPUs as streamprocessors, two major problems arise: data have to be transferred from the CPU main memory to the GPU main memory, which can be quite slow and the limited size of the GPU main memory. Furthermore, only when the streamprocessors are fully used to capacity, a remarkable speed-up comparing to a CPU is achieved. Therefore, new algorithms for the solution of optimal control problems are designed in this thesis. To this end, a nonoverlapping domain decomposition method is introduced which allows the exploitation of the computational power of many GPUs resp. CPUs in parallel. This algorithm is based on preliminary work for elliptic problems and enhanced for the application to optimal control problems. For the domain decomposition into two subdomains the linear system for the unknowns on the interface is solved with a Schur complement method by using a discrete approximation of the Steklov-Poincare operator. For the academic optimal control problem, the arising capacitance matrix can be inverted analytically. On this basis, two different algorithms for the nonoverlapping domain decomposition for the case of many subdomains are proposed in this thesis: on the one hand, a recursive approach and on the other hand a simultaneous approach. Numerical test compare the performance of the CSMG for the one domain case and the two approaches for the multi-domain case on a GPU and CPU for different variants.

The contribution of three genes (C15orf53, OXTR and MLC1) to the etiology of chromosome 15-bound schizophrenia (SCZD10), bipolar disorder (BD) and autism spectrum disorder (ASD) were studied. At first, the uncharacterized gene C15orf53 was comprehensively analyzed. Previous genome-wide association studies (GWAS) in bipolar disorder samples have identified an association signal in close vicinity to C15orf53 on chromosome 15q14. This gene is located in exactly the genomic region, which is segregating in our SCZD10 families. An association study with bipolar disorder (BD) and SCZD10 individual samples did not reveal any association of single nucleotide polymorphisms (SNPs) in C15orf53. Mutational analysis of C15orf53 in SCZD10-affected individuals from seven multiplex families did not show any mutations in the 5"-untranslated region, the coding region and the intron-exon boundaries. Gene expression analysis revealed that C15orf53 was expressed in a subpopulation of leukocytes, but not in human post-mortem limbic brain tissue. Summarizing these studies, C15orf53 is unlikely to be a strong candidate gene for the etiology of BD or SCZD10. The second investigated gene was the human oxytocin receptor gene (OXTR). Five well described SNPs located in the OXTR gene were taken for a transmission-disequilibrium test (TDT) in parents-child trios with ASD-affected children. Neither in the complete sample nor in a subgroup with children that had an intelligence quotient (IQ) above 70, association was found, independent from the application of Haploview or UNPHASED for analysis. The third gene, MLC1, was investigated with regards to its implication in the etiology of SCZD10. Mutations in the MLC1 gene lead to megalencephalic leukoencephalopathy with subcortical cysts (MLC) and one variant coding for the amino acid methionine (Met) instead of leucine (Leu) at position 309 was identified to segregate in a family affected with SCZD10. For further investigation of MLC1 and its possible implication in the etiology of SCZD10, a constitutive Mlc1 knockout mouse model should be created. Mouse embryonic stem cells (mES) were electroporated with a knockout vector construct and analyzed with respect to homologous recombination of the knockout construct with the genomic DNA (gDNA) of the mES. Polymerase chain reaction (PCR) on the available stem cell clones did not reveal any homologous recombined ES. Additionally, we conducted experiments to knockdown MLC1 and using microRNAs. The 3"-untranslated region of the MLC1 gene was analyzed with the bioinformatics tool TargetScan to screen for potential microRNA target sites. In the 3"-untranslated region of the MLC1 gene, a potential binding site for miR-137 was identified. The gene expression level of genes that had been linked to psychiatric disorders and carried a predicated miR-137 binding site has been proven to be immediately responsive to miR-137. Thus, there is new evidence that MLC1 is a candidate gene for the etiology of SCZD10.